Lignite Properties and Boiler Performance Energy Generation Conference: Reducing CO 2 Intensity in Power Plants Steve Benson Presented at the Energy Generation Conference Bismarck, ND January 28, 2015 1
Lignite Properties and Boiler Performance
Energy Generation Conference:Reducing CO2 Intensity in Power Plants
Steve BensonPresented at the Energy Generation Conference
Bismarck, ND January 28, 2015
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Contact InformationMicrobeam Technologies, Inc.
Email: [email protected]
North Dakota Office:4200 James Ray Drive, Ste. 193
Grand Forks, ND 58201Tel.: (701) 777-6530Fax: (701) 777-6532
Minnesota Office:14451 Hwy 7, Ste. 202
Minnetonka, MN Tel.: (701) 738-2447Fax: (763) 273-1347
Steve’s Cell: (701) 213-70702
Background of Microbeam Technologies, Inc. Mission: To provide advanced analysis and interpretations of the
impacts of fuel properties on plant fireside performance. Founded: 1991 and began performing analysis of samples using
advanced electron microscopy methods in 1992 Growth: Expanded laboratory in 2004 to include high-temperature
small scale test equipment – slag/ash behavior in combustion/gasification systems; New office in Minneapolis in 2014
Clients: Equipment developers, gasification (syngas, methane, fertilizers), electric utilities, state and federal government, coal companies, consultants, universities, law firms, research organizations, and others
Work: Conducted >1450 projects worldwide, >7000 samples analyzed
Staff: – experience with fossil/renewable fuels conversion and environmental control systems – research/development –commercialization – education – problem solving focus
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Overview Lignite Properties – Managing to improve performance Lignite Preparation Energy Conversion – Combustion/Boilers Fate of Lignite Impurities
Ash formation Slag Ash deposits – wall slagging and convective pass fouling Fine particulate
Boiler Design for Lignitic Coals Predictive Tools – use to improve performance and reduce
CO2 intensity Summary
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Lignite Properties High Moisture High oxygen content – organically
associated impurities Form and abundance of impurities – ash-
forming materials, sulfur High reactivity Non-caking
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Coal Impurities No ash in coal! – ash-forming components or
impurities Particles – minerals and other materials – Electron
microscopy – size, composition, abundance (3000 particles)
Inorganic elements associated with coal matrix –elements (alkali and alkaline earth elements) –Chemical fractionation – abundance of organically associated elements
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Sources of Impurities in Lignite During Formation From original plant material Influx of sand clays by wind and water Ground water flow Mineralization
During Mining Overburden, partings, underclay
incorporated into lignite
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Association of Impurities in Lignite
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Lignite Preparation
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Crushers and Pulverizers Cyclone Fired Boilers -3/8 in
Fluidized bed -1/4 in
Pulverized Coal 80% -200 mesh (74 µm)
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Impurities in Coal Higher mineral content Quartz and clays Ca organically
associated Clay mainly included
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Figure Point/Area Description Na Mg Al Si S K Ca Ti Fe Zr O 5 1 Excluded mineral 0.0 0.1 0.8 59.0 0.4 0.3 0.2 0.1 0.1 0.7 38.5
2 Included mineral 0.0 0.2 27.9 38.3 1.1 0.7 0.9 0.1 0.6 1.3 28.93 Included mineral 0.0 0.2 24.4 30.6 0.6 0.4 0.3 0.2 0.2 0.9 42.24 Excluded mineral 0.0 0.1 1.0 53.6 0.3 0.2 0.1 0.1 0.1 0.5 44.15 Excluded mineral 0.1 0.2 0.8 49.6 0.3 0.2 0.2 0.1 0.1 0.6 47.96 Included mineral 0.0 0.0 0.4 62.3 0.1 0.2 0.1 0.1 0.2 0.2 36.57 Included mineral 0.3 0.3 1.0 46.6 0.4 0.1 0.1 0.0 0.1 0.6 50.48 Coal matrix 0.0 0.0 2.7 4.9 18.7 1.4 42.1 1.9 4.9 3.4 20.19 Included mineral 0.0 0.0 0.5 23.8 0.2 0.1 0.2 0.1 0.2 55.2 19.9
6 1 Included mineral 0.0 0.1 26.6 31.8 0.3 0.2 0.2 0.1 0.3 0.6 39.92 Included mineral 0.0 0.0 9.2 49.2 0.4 5.8 1.3 2.6 3.1 0.2 28.33 Included mineral 0.0 0.1 18.1 41.4 2.6 10.3 4.5 2.5 2.4 2.2 15.94 Included mineral 1.1 1.2 2.6 40.6 1.2 0.5 1.1 0.1 0.2 1.5 50.05 Excluded mineral 0.1 0.0 0.7 88.4 0.0 0.4 0.4 0.3 0.4 0.1 9.36 Excluded mineral 0.0 0.0 0.7 60.0 0.2 0.2 0.1 0.1 0.2 0.5 38.07 Included mineral 0.0 0.0 0.7 57.6 0.0 0.2 0.3 0.3 0.4 0.1 40.38 Included mineral 0.1 0.4 22.2 36.2 2.4 1.3 1.8 0.2 0.5 2.3 32.69 Excluded mineral 3.2 1.0 22.2 29.1 0.8 3.0 0.8 0.7 0.8 0.9 37.6
Excluded Average 0.6 0.2 4.4 56.6 0.3 0.7 0.3 0.2 0.3 0.5 35.9Included Average 0.1 0.2 13.3 43.5 0.9 2.0 1.0 0.6 0.8 1.0 36.5
Mineral Types in Coal
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Conventional Analyses on CoalsOxides Antelope Rawhide Caballo ND Lignite
SiO2 25.6 28.3 26.7 21.2Al2O3 13.3 14.1 16.6 8.5Fe2O3 10.2 5.3 5.1 7.7TiO2 1.3 1.0 1.1 0.6P2O5 0.6 1.2 1.7 1.1CaO 24.8 27.3 25.1 19.6MgO 6.4 9.3 8.0 8.2Na2O 1.3 1.1 1.0 8.7K2O 0.1 0.3 0.3 0.4SO3 16.2 12.3 14.4 23.9
Moisture 23.5 30.7 29.7 36.8Vol. Matter 36.6 31.4 32.3 30.4Fixed Carbon 36.2 33.6 33.6 27.5Ash 3.8 4.4 4.5 5.4
Hydrogen 6.3 6.4 6.4 7.1Carbon 52.0 47.9 48.9 41.4Nitrogen 0.8 0.6 0.7 0.5Sulfur 0.3 0.3 0.3 0.6Oxygen 36.9 40.4 39.2 45.0Ash 3.8 4.4 4.5 5.3
Btu 8350 8262 8508 7252
Ash Composition,Wt % Equivalent Oxide
Proximate,Wt %
Ultimate,Wt %
Heating Value,BTU/lb
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Advanced Versus Conventional ASTM Analysis
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Energy Conversion Systems –Combustion - Boilers
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Overall Ash Formation and Deposition Processes
Benson, S.A., Jones, M.L. and Harb, J.N. Ash Formation and Deposition--Chapter 4. In: Fundamentals of Coal Combustion for Clean and Efficient Use, edited by Smoot, L.D. Amsterdam, London, New York, Tokyo: Elsevier, 1993, p. 299-373.
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Rocket Science?
Combustion – Pulverized Coal Flame – Test Burner
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Pulverized Coal Combustion Systems
Wall-fired (B, C) Tangential-fired (A)
Primary Air and Coal
Secondary Air
Primary Air and Coal
Secondary Air
Primary Air and Coal
Secondary Air
(A) (B) (C)
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Cyclone-Fired Coal Combustion Systems
Secondarysuperheater
Reheat superheater
Primary superheater
Economizer
Platers(suspended
surface)
Centrifugal Action
Secondary Air
Slag
Slag tap
CoalAir
Air
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Fate of Lignite Impurities
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Ash Formation in a Coal Flame
Molten Ash Droplets
Solid Particles
Na, K, SO2NOx, Hg etc.
Vapors
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Pulverized Coal Fired –Ash Formation Processes
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Transformations of Impurities in Boiler
• Size of ash particles• Composition of ash particles• Physical properties of ash particles• Deposits formation and collection of
ash particles
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Ash Formation – Partitioning
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Ash Particle Size and Composition Distribution
Na and Ca rich
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How do deposits form in boilers? Transport of particles and vapor phase
material to the surface Sticking to the surface – sticky material
formation
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Ash Transport to Heat Transfer Surfaces The transport of intermediate ash species
(inorganic vapors, liquids, and solids) is function of: State and size of the ash species System design – burner type, heat transfer
surface configuration System conditions, such as gas flow
patterns, gas velocity, and temperature
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Ash Transport Mechanisms
eddy
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Sticking and Bonding Phases
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Silicate Viscosity: Slag Flow, Particle Sticking, Deposit Strength
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Burners
Slagging
Convective pass fouling
High temperature
Low temperature
Wall Slagging (high-temperature bonding phases) Indicates propensity of
deposits to accumulate on the radiant walls of a boiler
Temperatures from 2000 to 3000°F (1093 to 1649°C).
Wall Slagging
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Deposit Thickness T-fired boiler
Ma, Inman, Lu, Sears, Kong, Rokanuzzaman, McCollor, Benson, Fuel Processing Technology 88 (2007) 1035–1043. 33
Burners
Slagging
Convective pass fouling
High temperature
Low temperature
Silicate (high temperature) Occurs in high-temperature
convective pass Temperatures between 1600 and
2400°F Silicate-based deposits
Sulfate (low temperature) Low-temperature convective pass Temperatures between 1000 and
1700°F Sulfate-based deposits
Convective Pass Fouling
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Deposit thickness (mm) on super heater division panel
Ma, Inman, Lu, Sears, Kong, Rokanuzzaman, McCollor, Benson, Fuel Processing Technology 88 (2007) 1035–1043.
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Convective pass deposits
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Deposit Sampling and Analysis
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Boiler Design for Lignite
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Effects of Rank and Coal Type on Boiler Sizing
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Important Design Criteria for the Furnace Net heat input per furnace plan area (Btu/hr-ft2) Vertical distance from top fuel nozzle to furnace arch
Distance is function of furnace width and depth Furnace dimensions must provide residence time to:
Properly burn fuel Cool the combustion products
Function of body of the boiler (radiative heat transfer)
Important Factors in Convective Pass Fouling Erosion can be diminished by minimizing gas velocities. Fouling can be reduced by:
Sootblowing- Air for low-fouling situations- Steam for high-fouling situations- Pulsed detonation - Acoustic horns
Lower heat release rates (large furnace volume) Greater number of wall blowers to minimize wall slagging Higher excess air levels Greater number of retractable sootblowers in the convective pass Increased tube spacing Additives
Convective Pass Design
Design Evolution for Boilers Firing North Dakota Lignite Coals
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Predictive Tools
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Ash Behavior IndicesExample
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Example: Predicted High-Temperature Fouling for Lignite Blends at four temperatures
Day 2 Lignite blendfired under 4 conditions
Day 3 Lignite blend fired under5 conditions
Day 4 Lignite blend fired Under 4 conditions
Day 1 BaselineLignite Blend
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Comparison of observed with predicted fouling behavior
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Summary - Lignite Property Impacts Moisture – lowers heating value, increases volume of gas in
combustor, changes where heat is absorbed Volatile matter – lower volatile matter decreases ability to stage
and reduce NOx Ash – increase lowers heating value
Higher basic ash (Na, Mg, Ca, K, Fe) (low ash contents) – fine particle formation, reflective ash in boiler, higher furnace exit gas temperatures, increased convective pass fouling, higher opacity
Higher acidic ash (Si, Al, Ti) (higher ash contents) – larger ash particle formation, wall slagging, high-temperature convective-pass fouling, lower low-temperature convective-pass fouling, lower opacity
Blending – significant opportunity to improve the efficiency/reliability and decrease CO2 intensity
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Contact InformationMicrobeam Technologies, Inc.
Email: [email protected]
North Dakota Office:4200 James Ray Drive, Ste. 193
Grand Forks, ND 58201Tel.: (701) 777-6530Fax: (701) 777-6532
Minnesota Office:14451 Hwy 7, Ste. 202
Minnetonka, MN Tel.: (701) 738-2447Fax: (763) 273-1347
Steve’s Cell: (701) 213-707049